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In vitro and in vivo superior radiosensitizing effect of berbamine for head and neck squamous cell carcinoma

BACKGROUND: Berbamine (BBM), one of the bis-benzylisoquinoline products isolated from Berberis amurensis, has been demonstrated for its anticancer effect against leukemia, breast cancer, liver cancer, etc. There are some studies focusing on the chemosensitization effect of BBM. However, there is no...

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Autores principales: Zhu, Hongmei, Ruan, Shu, Jia, Feng, Chu, Jiusheng, Zhu, Yong, Huang, Yongjiu, Liu, Guan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6241700/
https://www.ncbi.nlm.nih.gov/pubmed/30532553
http://dx.doi.org/10.2147/OTT.S171212
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author Zhu, Hongmei
Ruan, Shu
Jia, Feng
Chu, Jiusheng
Zhu, Yong
Huang, Yongjiu
Liu, Guan
author_facet Zhu, Hongmei
Ruan, Shu
Jia, Feng
Chu, Jiusheng
Zhu, Yong
Huang, Yongjiu
Liu, Guan
author_sort Zhu, Hongmei
collection PubMed
description BACKGROUND: Berbamine (BBM), one of the bis-benzylisoquinoline products isolated from Berberis amurensis, has been demonstrated for its anticancer effect against leukemia, breast cancer, liver cancer, etc. There are some studies focusing on the chemosensitization effect of BBM. However, there is no report about whether BBM could enhance the anticancer effect of radiation, which made us to explore the possible radiosensitization effect of BBM. MATERIALS AND METHODS: Here, in vitro cytotoxicity of BBM was evaluated on two kinds of head and neck squamous cancer cell lines. Clonogenic assay was performed to study the radiosensitization effect of BBM. Western blot was utilized to elucidate the possible mechanism underlying the radiosensitization effect. RESULTS: BBM effectively inhibited the growth of two kinds of cancer cells in a time- and dose-dependent manner. Radiation plus BBM led to significantly more reduction of the colony-forming ability of cancer cells when compared with radiation alone. BBM plus radiation led to the most reduction of STAT3 phosphorylation, followed by the significant decrease of the ratio of Bax/Bcl-2. In vivo study demonstrated that the combinational administration of BBM and radiation generated the most significant tumor-delaying effect among all of the treatment regimens. CONCLUSION: We reported, in the current study, the potential role of BBM in not only treating cancer by itself but also offering a promising way to improve the efficacy of radiotherapy by inhibiting the activation of STAT3 and subsequently inducing the apoptosis of cancer.
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spelling pubmed-62417002018-12-07 In vitro and in vivo superior radiosensitizing effect of berbamine for head and neck squamous cell carcinoma Zhu, Hongmei Ruan, Shu Jia, Feng Chu, Jiusheng Zhu, Yong Huang, Yongjiu Liu, Guan Onco Targets Ther Original Research BACKGROUND: Berbamine (BBM), one of the bis-benzylisoquinoline products isolated from Berberis amurensis, has been demonstrated for its anticancer effect against leukemia, breast cancer, liver cancer, etc. There are some studies focusing on the chemosensitization effect of BBM. However, there is no report about whether BBM could enhance the anticancer effect of radiation, which made us to explore the possible radiosensitization effect of BBM. MATERIALS AND METHODS: Here, in vitro cytotoxicity of BBM was evaluated on two kinds of head and neck squamous cancer cell lines. Clonogenic assay was performed to study the radiosensitization effect of BBM. Western blot was utilized to elucidate the possible mechanism underlying the radiosensitization effect. RESULTS: BBM effectively inhibited the growth of two kinds of cancer cells in a time- and dose-dependent manner. Radiation plus BBM led to significantly more reduction of the colony-forming ability of cancer cells when compared with radiation alone. BBM plus radiation led to the most reduction of STAT3 phosphorylation, followed by the significant decrease of the ratio of Bax/Bcl-2. In vivo study demonstrated that the combinational administration of BBM and radiation generated the most significant tumor-delaying effect among all of the treatment regimens. CONCLUSION: We reported, in the current study, the potential role of BBM in not only treating cancer by itself but also offering a promising way to improve the efficacy of radiotherapy by inhibiting the activation of STAT3 and subsequently inducing the apoptosis of cancer. Dove Medical Press 2018-11-14 /pmc/articles/PMC6241700/ /pubmed/30532553 http://dx.doi.org/10.2147/OTT.S171212 Text en © 2018 Zhu et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Zhu, Hongmei
Ruan, Shu
Jia, Feng
Chu, Jiusheng
Zhu, Yong
Huang, Yongjiu
Liu, Guan
In vitro and in vivo superior radiosensitizing effect of berbamine for head and neck squamous cell carcinoma
title In vitro and in vivo superior radiosensitizing effect of berbamine for head and neck squamous cell carcinoma
title_full In vitro and in vivo superior radiosensitizing effect of berbamine for head and neck squamous cell carcinoma
title_fullStr In vitro and in vivo superior radiosensitizing effect of berbamine for head and neck squamous cell carcinoma
title_full_unstemmed In vitro and in vivo superior radiosensitizing effect of berbamine for head and neck squamous cell carcinoma
title_short In vitro and in vivo superior radiosensitizing effect of berbamine for head and neck squamous cell carcinoma
title_sort in vitro and in vivo superior radiosensitizing effect of berbamine for head and neck squamous cell carcinoma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6241700/
https://www.ncbi.nlm.nih.gov/pubmed/30532553
http://dx.doi.org/10.2147/OTT.S171212
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